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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:C18orf25-FXR1 (FusionGDB2 ID:11134)

Fusion Gene Summary for C18orf25-FXR1

check button Fusion gene summary
Fusion gene informationFusion gene name: C18orf25-FXR1
Fusion gene ID: 11134
HgeneTgene
Gene symbol

C18orf25

FXR1

Gene ID

147339

8087

Gene namechromosome 18 open reading frame 25FMR1 autosomal homolog 1
SynonymsARKL1|Ark2N|RNF111L1FXR1P
Cytomap

18q21.1

3q26.33

Type of geneprotein-codingprotein-coding
Descriptionuncharacterized protein C18orf25ARKadia-like 1ARKadia-like protein 1fragile X mental retardation syndrome-related protein 1fragile X mental retardation, autosomal homolog 1
Modification date2020031320200320
UniProtAcc

Q96B23

P51114

Ensembl transtripts involved in fusion geneENST00000282059, ENST00000321319, 
ENST00000445140, ENST00000468861, 
ENST00000480918, ENST00000491062, 
ENST00000491674, ENST00000305586, 
ENST00000357559, 
Fusion gene scores* DoF score9 X 6 X 5=2709 X 11 X 4=396
# samples 911
** MAII scorelog2(9/270*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/396*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: C18orf25 [Title/Abstract] AND FXR1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC18orf25(43833786)-FXR1(180693914), # samples:1
Anticipated loss of major functional domain due to fusion event.C18orf25-FXR1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
C18orf25-FXR1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgeneFXR1

GO:2000637

positive regulation of gene silencing by miRNA

17057366


check buttonFusion gene breakpoints across C18orf25 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across FXR1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/AAV746723C18orf25chr18

43833786

+FXR1chr3

180693914

+


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Fusion Gene ORF analysis for C18orf25-FXR1

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-intronENST00000282059ENST00000445140C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000282059ENST00000468861C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000282059ENST00000480918C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000282059ENST00000491062C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000282059ENST00000491674C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000321319ENST00000445140C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000321319ENST00000468861C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000321319ENST00000480918C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000321319ENST00000491062C18orf25chr18

43833786

+FXR1chr3

180693914

+
5CDS-intronENST00000321319ENST00000491674C18orf25chr18

43833786

+FXR1chr3

180693914

+
Frame-shiftENST00000282059ENST00000305586C18orf25chr18

43833786

+FXR1chr3

180693914

+
Frame-shiftENST00000282059ENST00000357559C18orf25chr18

43833786

+FXR1chr3

180693914

+
Frame-shiftENST00000321319ENST00000305586C18orf25chr18

43833786

+FXR1chr3

180693914

+
Frame-shiftENST00000321319ENST00000357559C18orf25chr18

43833786

+FXR1chr3

180693914

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for C18orf25-FXR1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
C18orf25chr1843833786+FXR1chr3180693909+2.35E-070.99999976
C18orf25chr1843833786+FXR1chr3180693909+2.35E-070.99999976

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.
genomic feature of top 1%

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Fusion Protein Features for C18orf25-FXR1


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:43833786/:180693914)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
C18orf25

Q96B23

FXR1

P51114

FUNCTION: RNA-binding protein required for embryonic and postnatal development of muscle tissue (PubMed:30770808). May regulate intracellular transport and local translation of certain mRNAs (By similarity). {ECO:0000250|UniProtKB:Q61584, ECO:0000269|PubMed:30770808}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for C18orf25-FXR1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for C18orf25-FXR1


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for C18orf25-FXR1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for C18orf25-FXR1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource